V-SPERM WASH
K-Number: K223117 · 2023-01-31
Device Summary
Frequently Asked Questions
What is the V-SPERM WASH?
V-SPERM WASH is a medical device that received FDA 510(k) clearance on 2023-01-31. The listed applicant is Vitromed GmbH. The 510(k) number is K223117.
When did V-SPERM WASH receive FDA 510(k) clearance?
V-SPERM WASH received FDA 510(k) clearance on 2023-01-31, under 510(k) number K223117.
Who is the listed applicant for V-SPERM WASH?
The FDA 510(k) record lists Vitromed GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for V-SPERM WASH?
The FDA product code for V-SPERM WASH is MQL.
Other records listing Vitromed GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.